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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895572Generated: October 31, 2026

Chloranil → HCID 58289111, compound

https://huagongshe.com/reaction/1895572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloranilHCID 8371—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178477814HCID 178477814—
SolventBenzeneHCID 241—
ProductHCID 58289111HCID 5828911117%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2,3,9,10-tetrachloro-trans-6,13-bis(phenylethylthio)-6,13-dihydropentacene (0.3 g, 0.44 mmol), tetrachloro-1,4-benzoquinone (0.22 g, 0.89 mmol) and potassium carbonate (0.61 g, 4.45 mmol) in dry benzene (50 mL) was stirred at 60° C. for 48 h under an argon atmosphere in the dark. After cooling to RT, the reaction mixture was filtered and washed with CH2Cl2. After evaporation of the filtrate, the solid residue was passed through short column of n-Al2O3 eluted with CH2Cl2 and the deep blue band was collected. The solvent was evaporated to give pure 2,3,9,10-tetrachloro-6,13-bis(phenethylthio)pentacene as deep blue solids in 17% yield (0.05 g). 1H NMR (500 MHz, CDCl3): δ 9.48 (s, 4H), 8.11 (s, 4H), 7.24 (m, 6H), 7.06 (m, 4H), 3.27 (t, 4H, J=7.32 Hz), 2.85 (t, 4H, J=7.32 Hz). 13C NMR (125.68 MHz, CDCl3): δ 132.89, 132.44, 132.25, 128.95, 128.73, 128.59, 127.07, 126.56, 126.14, 38.04, 36.53. LDI-MS m/z: 688 [M+], UV-vis λmax(nm): 628, 577, 537.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513466B2
Source datasetuspto-grants-2013_08
ORD IDord-1d0c7131bcfe45b681c3bdb82ceb2952
Source noteuspto-grants-2013_08